Supporting Information
Supporting Information File 1: Experimental procedures, spectra of new compounds, CIF data, and details of the computational study. | ||
Format: PDF | Size: 2.3 MB | Download |
Cite the Following Article
Pyridylidene ligand facilitates gold-catalyzed oxidative C–H arylation of heterocycles
Kazuhiro Hata, Hideto Ito, Yasutomo Segawa and Kenichiro Itami
Beilstein J. Org. Chem. 2015, 11, 2737–2746.
https://doi.org/10.3762/bjoc.11.295
How to Cite
Hata, K.; Ito, H.; Segawa, Y.; Itami, K. Beilstein J. Org. Chem. 2015, 11, 2737–2746. doi:10.3762/bjoc.11.295
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Díaz-Salazar, H.; Medina-Mercado, I.; Salvador-Reyes, R.; Barquera-Lozada, J. E.; Martínez-Otero, D.; Porcel, S. Oxy- and Chloroarylation Pathways in Gold-Mediated Cyclization of 2-Aminoaryl-3-arylpropargyl-benzenesulfonamides. Chemistry (Weinheim an der Bergstrasse, Germany) 2023, 29, e202302074. doi:10.1002/chem.202302074
- Joo, J. M. doi:10.1002/9781119774167.ch3
- Segawa, Y. Nonplanar Aromatic Hydrocarbons: Design and Synthesis of Highly Strained Structures. Bulletin of the Chemical Society of Japan 2022, 95, 1600–1610. doi:10.1246/bcsj.20220270
- Koyioni, M.; Koutentis, P. A. doi:10.1002/9783527834242.chf0219
- Urvashi, X.; Singh, P.; Patil, N. T. doi:10.1002/9783527834242.chf0100
- Madhavan, S.; Keshri, S. K.; Kapur, M. Transition Metal-Mediated Functionalization of Isoxazoles: A Review. Asian Journal of Organic Chemistry 2021, 10, 3127–3165. doi:10.1002/ajoc.202100560
- Minami, Y.; Hiyama, T. Cross-coupling Reaction based on the Transformation of Trialkylsilyl Groups. Journal of Synthetic Organic Chemistry, Japan 2021, 79, 642–651. doi:10.5059/yukigoseikyokaishi.79.642
- Praveen, C.; Dupeux, A.; Michelet, V. Catalytic Gold Chemistry: From Simple Salts to Complexes for Regioselective C-H Bond Functionalization. Chemistry (Weinheim an der Bergstrasse, Germany) 2021, 27, 10495–10532. doi:10.1002/chem.202100785
- China, H.; Kageyama, N.; Yatabe, H.; Takenaga, N.; Dohi, T. Practical Synthesis of 2-Iodosobenzoic Acid (IBA) without Contamination by Hazardous 2-Iodoxybenzoic Acid (IBX) under Mild Conditions. Molecules (Basel, Switzerland) 2021, 26, 1897. doi:10.3390/molecules26071897
- Tsuda, M.; Morita, T.; Fukuhara, S.; Nakamura, H. Synthesis of 4-amino-5-allenylisoxazoles via gold(I)-catalysed propargyl aza-Claisen rearrangement. Organic & biomolecular chemistry 2021, 19, 1358–1364. doi:10.1039/d0ob02544e
- Zheng, Z.; Ma, X.; Cheng, X.; Zhao, K.; Gutman, K.; Li, T.; Zhang, L. Homogeneous Gold-Catalyzed Oxidation Reactions. Chemical reviews 2021, 121, 8979–9038. doi:10.1021/acs.chemrev.0c00774
- Fricke, C.; Reid, W. B.; Schoenebeck, F. A Review on Oxidative Gold-Catalyzed C-H Arylation of Arenes – Challenges and Opportunities. European Journal of Organic Chemistry 2020, 2020, 7119–7130. doi:10.1002/ejoc.202000856
- Whyte, A.; Torelli, A.; Mirabi, B.; Zhang, A.; Lautens, M. Copper-Catalyzed Borylative Difunctionalization of π-Systems. ACS Catalysis 2020, 10, 11578–11622. doi:10.1021/acscatal.0c02758
- Ball, L. T.; Corrie, T. J. A.; Cresswell, A. J.; Lloyd-Jones, G. C. Kinetic Analysis of Domino Catalysis: A Case Study on Gold-Catalyzed Arylation. ACS Catalysis 2020, 10, 10420–10426. doi:10.1021/acscatal.0c03178
- 英人, 伊.; 和, 松.; 裕太, 矢.; 万織, 柴.; 健一郎, 伊. 縮環π拡張(APEX)反応による多環芳香族化合物の精密合成. Journal of Synthetic Organic Chemistry, Japan 2020, 78, 671–682. doi:10.5059/yukigoseikyokaishi.78.671
- Nottingham, C.; Barber, V.; Lloyd‐Jones*, G. C. doi:10.1002/0471264229.os096.11
- Morita, T.; Fuse, S.; Nakamura, H. Photochemical Conversion of Isoxazoles to 5-Hydroxyimidazolines. Organic letters 2020, 22, 3460–3463. doi:10.1021/acs.orglett.0c00910
- Kramer, S. Homogeneous Gold-Catalyzed Aryl–Aryl Coupling Reactions. Synthesis 2020, 52, 2017–2030. doi:10.1055/s-0039-1690882
- Panigrahi, A.; Whitaker, D.; Vitorica-Yrezabal, I. J.; Larrosa, I. Ag/Pd Cocatalyzed Direct Arylation of Fluoroarene Derivatives with Aryl Bromides. ACS catalysis 2020, 10, 2100–2107. doi:10.1021/acscatal.9b05334
- Medina-Mercado, I.; Asomoza-Solís, E. O.; Martínez-González, E.; Ugalde-Saldívar, V. M.; Ledesma-Olvera, L. G.; Barquera-Lozada, J. E.; Gómez-Vidales, V.; Barroso-Flores, J.; Frontana-Uribe, B. A.; Porcel, S. Ascorbic Acid as an Aryl Radical Inducer in the Gold Mediated Arylation of Indoles with Aryldiazonium Chlorides. Chemistry (Weinheim an der Bergstrasse, Germany) 2019, 26, 634–642. doi:10.1002/chem.201904413